ZMP
syn1
Ensembl ID:
ZFIN ID:
Description:
synapsin-1 [Source:RefSeq peptide;Acc:NP_001119909]
Human Orthologue:
SYN1
Human Description:
synapsin I [Source:HGNC Symbol;Acc:11494]
Mouse Orthologue:
Syn1
Mouse Description:
synapsin I Gene [Source:MGI Symbol;Acc:MGI:98460]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21334 | Nonsense | Available for shipment | Available now |
| sa7143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14827 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34436 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa12369 | Nonsense | Available for shipment | Available now |
| sa21335 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21334
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 212 | 670 | 5 | 13 |
| ENSDART00000136578 | Nonsense | 212 | 670 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31976751)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31119477 |
| GRCz11 | 8 | 31128709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATATATGTCTCGATGTGATTGTTTGTTCTTTCAGTTCTCTCAGTTGTCC[A/T]GATTGTACAAGCAGTTGGGTCCAGAGGAGTTCCCACTGATCGACCAGGTT
Long Flanking Sequence:
TTGCAATAAAAAAAGATATATGTGTGTGGCACTAAAACTCTTTTAGGGCACATTGTGATATAAATGAGATATTTATAATTTTATTCTAAGTACATTATAATATTATTAATACAATTCAAGCATTTTTTTCTGTATGTCTCAAATATTAAATTAGGAAGTTATCATGGCAACTTTAATGTAATACAGTTCGAAATATTTAGGCCCACCACCCCTCAAACAAGTTTGGGCACCCCTGCTATAAAGCAACACATACACACACTTATACTTGTTAAAGCAACTTTTTCTGCAGCTTAGATCAATAATGGAATAATACTGTATAAAAGCTTTTAGGAAAATTTGATACCATCACAAGCCTGGAATTATTTCTTAAACATGAATTCAACAGGTTGACAACATTCTCTGATGCATCTCCAGTTATAGTTGCACCTATATTATTCCTTATTGCTCTATAATATATGTCTCGATGTGATTGTTTGTTCTTTCAGTTCTCTCAGTTGTCC[A/T]GATTGTACAAGCAGTTGGGTCCAGAGGAGTTCCCACTGATCGACCAGGTTTACTACCCCAACCACAAGGAGATGGTGAGTGTTAACCATCTGTCCCTCTCCTCGCTAGTAAACCCTGAGCTATAGGACACTAGACGGTCCCTCTGGACCCAATACAAAGCCTTCATCCGTGGAAGGGACAGCGGTGCCTGGACTTCGTACACAGTAAAATCTAAAAGGTTCATGCATATACAGTGCCCCAGTGAAGTGCTGCTCCACTCAACTTAGCACAGTCCTGTCTAGACCGGAAATTTTATAACCCCCAGACTGGTATAATTGCTTGGTGCATCATAGTCCTTATAGACACAGTTCAGGTTTTATTAGGAGAGGAAGCCTTACTGCAGTGCCACCACCTCCTCCTATTTCTCCACTGCAGGCATCTTCACACATAAATGATCCCAGACACAGTCTCCGGCAGAATGTTTTCCTCTCTCACTGGCCTTTTTTTTAAGATAAAGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7143
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 289 | 670 | 7 | 13 |
| ENSDART00000136578 | Nonsense | 289 | 670 | 8 | 14 |
| ENSDART00000084969 | Nonsense | 289 | 670 | 7 | 13 |
| ENSDART00000136578 | Nonsense | 289 | 670 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31979404)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31122130 |
| GRCz11 | 8 | 31131362 |
KASP Assay ID:
554-5053.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTGGCTTTGACAAAGACGTATGCCACATCTGAGCCTTTTATTGATGCC[A/T]AGTATGACATCCGAATCCAGAAAATTGGGGAAAATTACAAGGCCTACATG
Long Flanking Sequence:
TATCAAAAATGCTTCTGCAATAATGTCATGCCAATATAGCAACTTGAGAGAGAGCGAGAGAGAGGTAATAGGTGCTGTGGGTAATAAGTGTTTCAATCCGGCTTTACCACCGCAAGTATATTTCAAACCTGTGGGAAACACTGTGTGTCTCTAAATACTTTTAAAATAAATTGCTCTCTTGTCATTAGATTACTACACCTGGCTTTCCTGTGGTAGTGAAGATGGGTCATGCTCATTCTGGCATGGGAAAGGTATGAATGAAATAATTTCTTTAATGTTTATATTAACTGCTGTTTAGATATATATGACCAGTTACATTATTGATTTCATTAATTACATTTGCACATAAATCAAAGCACAAACTATCTATATTACCATATGACTAGTTCAGTCTTTTTCCTGTACAGGTCAAAGTAGACAATCAGTATGATTTCCAAGACATTGCTAGTGTTGTGGCTTTGACAAAGACGTATGCCACATCTGAGCCTTTTATTGATGCC[A/T]AGTATGACATCCGAATCCAGAAAATTGGGGAAAATTACAAGGCCTACATGTAAGAGATTTTAGCCACTATATTATTCTGGTTTCAAACATCATCTTTTGCACTTGCATTATAATTGGAACGGATTGTGAGACACTGTGTCATTCCTGCTGTTGTGTTATTGGACAGGAGGACATCCATATCTGGCAACTGGAAGACCAACACAGGATCAGCCATGCTGGAGCAGGTGGCCATGTCTGACAGGTACATACATCTTATAAAAATCTTATTCTGCCATTATGCAAAACTTCTGTAATATAACATTAGATAGGCCTTTTAGACATTTGGTTGTCTAAAAAAACATATTTAGTGTAATTTAACATTAGTAACACATACTATATGATCATTTCTCTTTTTTTTTGACATGCTTCCTCTCATGACAGCTAACTGCAGGTTAATTCTATAGCAGCATCACATTATCATTCAAAATAAAAAATGAAGTTAAAAAAATGACATGCACGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14827
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 289 | 670 | 7 | 13 |
| ENSDART00000136578 | Nonsense | 289 | 670 | 8 | 14 |
| ENSDART00000084969 | Nonsense | 289 | 670 | 7 | 13 |
| ENSDART00000136578 | Nonsense | 289 | 670 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31979404)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31122130 |
| GRCz11 | 8 | 31131362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTGGCTTTGACAAAGACGTATGCCACATCTGAGCCTTTTATTGATGCC[A/G]AGTATGACATCCKAATCCAGAAAATTGGGGAMAATTACAAGGCCTACATG
Long Flanking Sequence:
TATCAAAAATGCTTCTGCAATAATGTCATGCCAATATAGCAACTTGAGAGAGAGCGAGAGAGAGGTAATAGGTGCTGTGGGTAATAAGTGTTTCAATCCGGCTTTACCACCGCAAGTATATTTCAAACCTGTGGGAAACACTGTGTGTCTCTAAATACTTTTAAAATAAATTGCTCTCTTGTCATTAGATTACTACACCTGGCTTTCCTGTGGTAGTGAAGATGGGTCATGCTCATTCTGGCATGGGAAAGGTATGAATGAAATAATTTCTTTAATGTTTATATTAACTGCTGTTTAGATATATATGACCAGTTACATTATTGATTTCATTAATTACATTTGCACATAAATCAAAGCACAAACTATCTATATTACCATATGACTAGTTCAGTCTTTTTCCTGTACAGGTCAAAGTAGACAATCAGTATGATTTCCAAGACATTGCTAGTGTTGTGGCTTTGACAAAGACGTATGCCACATCTGAGCCTTTTATTGATGCC[A/G]AGTATGACATCCGAATCCAGAAAATTGGGGAAAATTACAAGGCCTACATGTAAGAGATTTTAGCCACTATATTATTCTGGTTTCAAACATCATCTTTTGCACTTGCATTATAATTGGAACGGATTGTGAGACACTGTGTCATTCCTGCTGTTGTGTTATTGGACAGGAGGACATCCATATCTGGCAACTGGAAGACCAACACAGGATCAGCCATGCTGGAGCAGGTGGCCATGTCTGACAGGTACATACATCTTATAAAAATCTTATTCTGCCATTATGCAAAACTTCTGTAATATAACATTAGATAGGCCTTTTAGACATTTGGTTGTCTAAAAAAACATATTTAGTGTAATTTAACATTAGTAACACATACTATATGATCATTTCTCTTTTTTTTTGACATGCTTCCTCTCATGACAGCTAACTGCAGGTTAATTCTATAGCAGCATCACATTATCATTCAAAATAAAAAATGAAGTTAAAAAAATGACATGCACGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34436
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 359 | 670 | 9 | 13 |
| ENSDART00000136578 | Nonsense | 359 | 670 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31983733)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31126459 |
| GRCz11 | 8 | 31135691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGGGGTCTCGATATATGCGCTGTTGAAGCACTGCATGGTAAAGACGGT[C/T]GAGATTACATAATAGAGGTAATGACATCTGCAAAAACAGGCAGCTTTTAA
Long Flanking Sequence:
GAATTCTCCCGATCCTCCCGATTAGCCAATCCGGGCCTGAGTGGGTCTATTCAATCATTAGCCTAACTTTGTGCTATTCTTAGACGTCTATTAGATCTTGACTGACAGCCCCCAAAATCAGCCTTGTTTTAGCCAAGACATCCACGCTAGACGTCTATTTGATTTCTAATAAACACAAAATGAATTGTCACATCTGATGTTTTAAACAGATATATCCCACATTTAAATCAGGTCAGTTTGTTCCATGTTTAGATTACATTTAAATCTAAACAGTCAATGACCCCTAGTCAAATATTAGTGTCTTGCACTGCAGTGATCCTGATTCCCTTGTTTGCTCTGGGTAGTGTACTGTTGGTGTGGGTGGCTGCTTTTAGTGGAATACACAAGGTCATCATTTGCACTTTTTCCCCTGCAGGTATCGTATGTGGGTGGATGTGTGCTCGGAGGTCTTTGGGGGTCTCGATATATGCGCTGTTGAAGCACTGCATGGTAAAGACGGT[C/T]GAGATTACATAATAGAGGTAATGACATCTGCAAAAACAGGCAGCTTTTAAAAGAATTAAACATATGCTTAGTGCCCTAGGCAAGCGCTCATTTCTGTCTCTTTCTGTGTTTGTTTATTAGGTGGTGGGCTGCTCAATGCCTCTGATTGGAGACCAGCAGGATGAGGACCGGGCTCTCATGGCTGACCTTGTTGTGGCTAAAATGAACGAGACAGTGCCACGCACTTCAGCTCCCACTACAGTCCGTTCTCAGGTTAACACTCTCACTTCAAAACATGCTCAAACTAAGCTCACTGGATATATGTGCATTCTAAATTATATCATGTTGTTTTTTGGAACATTTTGTGATGCAAACAAAGTAAAATGCTTAATTGTAGGCTCTAAATGCAAAATTTATAAGAAAGTTTTAATGTTAAGTTTTATTAGAAACAAATGAATGTAAATCTGGAATGCTTTCTTATGTTTGTTGCACTTAAAGATACAGTCAGAAAGAACAGTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12369
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 480 | 670 | 12 | 13 |
| ENSDART00000136578 | Nonsense | 480 | 670 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31990192)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31132918 |
| GRCz11 | 8 | 31142150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCAATCCCAGTCTGTGACCAGCCCTATTGCTCAGAATCCACCTGCTCAA[C/T]AACCGCGGCCCAATCAACCGCCCCAGCGACAGGCCAGTCAAGGTTCAGCA
Long Flanking Sequence:
ATTTTTTGGTATTTGTTATGCAGCAAGCCCAGAGATTGTTGTGTACACTTTGGTTTTATATAAAAGTAACTTTAATGTGTGATAGGAATAAAACGTGGTCATATACGAATGATTTCTCCACTCAATGAATGGCGGCTTGGACCCGGAAACAGTATTACATACGTCACAAACACGTCACCACTTAACAAGCGGATACTTGCTACCCCCACTCTTTATTCTCTGCTGAATTGCAGAAGTCATTTGTAATATTATAAATGTCCTTATTTATCGTATATTTGACGAAAGCTGTTTACTTCACCAGCAAAATGAAGCAGATATTCCAACTATATTTTGCCCTGTAAGAATGAGCTCTTGTTTTAGGAGGCCCTCAACAAGCTGCTGCTAGCACTGCTGCTACCCGTCAAGGAGCACCACCACAGCAGCGGCCCTCTCCTCAAGGCCAGCCTCCTGCCCAATCCCAGTCTGTGACCAGCCCTATTGCTCAGAATCCACCTGCTCAA[C/T]AACCGCGGCCCAATCAACCGCCCCAGCGACAGGCCAGTCAAGGTTCAGCAGCTCCACAGAGGCCTCCTGCAGCACAGATACCTGCTCAGCGTGGCTCTCCTCAGTCACAGAGGCAAGGCGGACCCCAACAAGGTGGTCCTCAAACTGGTGGTCAGAGTCCCAAACCAGCCGGTCAGCCCCAACAGAGGCCTCAGCAGCCAAGACAAGGCCAGCCAACCAGGCAGCCTACCCAGGGTGGCCCACAGCAGACCCAGGACGCCCCACAGCCAGCCCCGCAAGGCAGTCCTCGTCCTCCTACCACACAACAACCACGGCCTACTGCACCGGGACAGGGAGGCCCAGGAGGCACACGCCCTCCCTTGCAGCAGAAACCCCAACCTCCACAGAAACCCAGTCCTGATCACCCTGCCTTGAGTGGATCACCGCAGCTTAAGTAAGATGTTTTTTGTCCTCTGTGTAATCGGCTTGAAAATGATAGGTTCCACTCACTGGATGTGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21335
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000084969 | Nonsense | 608 | 670 | 12 | 13 |
| ENSDART00000136578 | Nonsense | 608 | 670 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 31990576)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 31133302 |
| GRCz11 | 8 | 31142534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGCCCAGGAGGCACACGCCCTCCCTTGCAGCAGAAACCCCAACCTCCA[C/T]AGAAACCCAGTCCTGATCACCCTGCCTTGAGTGGATCACCGCAGCTTAAG
Long Flanking Sequence:
GCACTGCTGCTACCCGTCAAGGAGCACCACCACAGCAGCGGCCCTCTCCTCAAGGCCAGCCTCCTGCCCAATCCCAGTCTGTGACCAGCCCTATTGCTCAGAATCCACCTGCTCAACAACCGCGGCCCAATCAACCGCCCCAGCGACAGGCCAGTCAAGGTTCAGCAGCTCCACAGAGGCCTCCTGCAGCACAGATACCTGCTCAGCGTGGCTCTCCTCAGTCACAGAGGCAAGGCGGACCCCAACAAGGTGGTCCTCAAACTGGTGGTCAGAGTCCCAAACCAGCCGGTCAGCCCCAACAGAGGCCTCAGCAGCCAAGACAAGGCCAGCCAACCAGGCAGCCTACCCAGGGTGGCCCACAGCAGACCCAGGACGCCCCACAGCCAGCCCCGCAAGGCAGTCCTCGTCCTCCTACCACACAACAACCACGGCCTACTGCACCGGGACAGGGAGGCCCAGGAGGCACACGCCCTCCCTTGCAGCAGAAACCCCAACCTCCA[C/T]AGAAACCCAGTCCTGATCACCCTGCCTTGAGTGGATCACCGCAGCTTAAGTAAGATGTTTTTTGTCCTCTGTGTAATCGGCTTGAAAATGATAGGTTCCACTCACTGGATGTGAAGGTTTCGATGATTCATAAGCATTTGGACATGTTTTTCTATTGATTGATGTTGTTTCGTAACCCATGCGAGTGAATACACCAGATGGTGCCCATTTTTCTCAGCTGTGCCTCAAATTGCATGACAAGATGATGGTATGATTGACAGTGGCTGTGTGAATTAGAGTAAAGCTATTAAGGTTAAATACAAACTTCAAAAATAGATGTATTCAGATTTAATTGCACTGAGCGCCTAATTTTGGGATCGGAACAACCAAAAATGTCATTTTGGGGTGGAGGAGAGATGATGTGAAATGGGACACAGAGGTCAGTTATGGCTAAATATATAGGTCTCCTCTTGTGCTAATTATTTGGATTATACCTGAACTTGGATCTCCTGACCTTGGTT
Associated Phenotype:
Not determined